FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Implant-One System

K Number: K173701 · Decision Nov 29, 2018
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
360

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Basic Information

Device Name
Implant-One System
K Number
K173701
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implant Logistics, Inc.
Date Received
December 4, 2017
Decision Date
November 29, 2018
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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Other Clearances by Implant Logistics, Inc.

K Number Device Name
K231455 Implant-One System
K212394 Implant-One Multi-Unit Abutment